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Freelance QA Consultant - Medical Devices

Initia Ltd.Petah Tikva, Center District, IsraelNot specifiedFull-timeSeniority: Not specified

Posted 13 days ago · 0 applicants

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The role in plain words

Must-have
  • Strong knowledge of ISO 13485
  • Strong knowledge of UK MDR
Nice-to-have

    Extracted from the job description · kept up to date automatically

    Who this suits

    Full job description

    Original listing · kept for reference

    We are looking for an experienced QA Consultant to support our medical device company on a part-time freelance basis.

    Immediate need:

    Conduct internal audits in accordance with ISO 13485 and UK MDR requirements.

    Assess audit readiness and identify compliance gaps.

    Provide recommendations and support corrective actions as needed.

    Requirements:

    Provide recommendations and support corrective actions as needed.

    Preferred experience:

    Proven experience in medical device Quality Assurance.

    Strong knowledge of ISO 13485 and UK MDR.

    Experience leading and conducting internal audits.

    This engagement is expected to start with internal audit activities, with the potential to expand into additional Quality and Regulatory support in the future.

    This position is open to all candidates.

    About Initia Ltd.
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    Questions about this role

    • This listing did not state a salary. We only show pay when the employer publishes it.
    Initia Ltd.
    Posted 13 days ago · 0 applicants
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